DEVICE: SAPIEN 3 Ultra System (00690103207828)
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If so, send a picture of the label to
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Device Identifier (DI) Information
SAPIEN 3 Ultra System
9750CM23
In Commercial Distribution
9750CM23A
Edwards Lifesciences LLC
9750CM23
In Commercial Distribution
9750CM23A
Edwards Lifesciences LLC
SAPIEN 3 Ultra valve with Commander delivery System
Device Characteristics
| MR Conditional | |
| No | |
| No | |
| Yes | |
| Yes | |
| No | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 60245 | Aortic transcatheter heart valve bioprosthesis, stent-like framework |
An implantable xenograft (e.g., bovine, porcine) intended to be used to repair/replace a stenosed and/or regurgitant aortic heart valve, or previously-implanted aortic heart valve prosthesis, and which is designed to be implanted with a catheter via transarterial access (e.g., femoral, subclavian, aortic) or transapical access while the heart is beating. It is comprised of the xenograft, processed to render the tissue non-viable, attached to an expandable metal framework, which is implanted with an included catheter, and when in situ, may be expanded with a balloon or self-expand. Typically devices associated with implantation (e.g., catheter, introducer) are included.
|
Active | true |
| 60246 | Mitral transcatheter heart valve bioprosthesis |
An implantable xenograft (e.g., bovine) intended to be used to repair/replace a stenosed or regurgitant mitral heart valve, or previously-implanted mitral heart valve prosthesis, and which is implanted with a catheter via percutaneous access (e.g., transfemoral, transapical) while the heart is beating. It is comprised of the xenograft, processed to render the tissue non-viable, attached to a metal framework (which may be covered with a synthetic polymer material) that is expandable in situ; it may also include a synthetic polymer subannular valve anchoring component. Devices to assist implantation (e.g., catheter, introducer) are typically included.
|
Active | true |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| NPU | Prosthesis, Mitral Valve, Percutaneously Delivered |
| NPT | Aortic Valve, Prosthesis, Percutaneously Delivered |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| P140031 | 091 |
| P140031 | 104 |
| P140031 | 107 |
| P140031 | 112 |
| P140031 | 146 |
| P140031 | 182 |
| P140031 | 186 |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Special Storage Condition, Specify: The delivery system should be stored in a cool, dry place. |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Outer Diameter: 23.0000 Millimeter |
Device Record Status
f792b4d5-ca30-4727-9ead-08a37a2e6f33
September 22, 2026
9
August 30, 2019
September 22, 2026
9
August 30, 2019
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| No Package DIs found | |||||
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)822-9637
tech_support@edwards.com
tech_support@edwards.com